1721-59-1|Diplopterol|22-Hydroxyhopane|-范德生物科技公司

Diplopterol

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names：
22-Hydroxyhopane
CAS号：
1721-59-1
MDL Number：
MF(分子式)： C30H52O MW(分子量)： 428.75
EINECS: Reaxys Number:
Pubchem ID: Brand:BIOFOUNT

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中文别名	Diplopterol
英文别名	Diplopterol
CAS号	1721-59-1
SMILES	CC1(C)CCC[C@]2(C)[C@@]3([H])CC[C@]4([H])[C@@]5(C)CC[C@H](C(C)(O)C)[C@@]([H])5CC[C@](C)4[C@@](C)3CCC12
Inchi	InChI=1S/C30H52O/c1-25(2)15-9-16-28(6)22(25)14-19-30(8)24(28)11-10-23-27(5)17-12-20(26(3,4)31)21(27)13-18-29(23,30)7/h20-24,31H,9-19H2,1-8H3/t20-,21-,22?,23+,24+,27-,28-,29+,30+/m0/s1
InchiKey	PNJBOAVCVAVRGR-INNBTYQQSA-N
分子式 Formula	C30H52O
分子量 Molecular Weight	428.75
闪点 FP
熔点 Melting point
沸点 Boiling point
Polarizability极化度
密度 Density
蒸汽压 Vapor Pressure
溶解度Solubility
性状	Solid powder
储藏条件 Storage conditions	Dry, dark and store at 0-4℃ for short term (days to weeks) or -20℃ for long term (Store correctly 2-3years).

产品说明	Diplopterol(CAS:1721-59-1):仅限应用于工业或者科学研究过程中非医疗目的，不应用于人类或动物的临床诊断以及治过程疗，该产品非药用，非食用。
Introduction	Diplopterol is a biosyntheside from squalene in a cell-free system for Acetobacter pasteurianum. It is a hopanoid that can function as a substitute for sterols.
Application1
Application2
Application3

警示图
危险性	Warning
危险性警示
安全声明
安全防护
备注

[1]Wu CH, Kong L, Bialecka-Fornal M, Park S, Thompson AL, Kulkarni G, Conway SJ, Newman DK. Quantitative hopanoid analysis enables robust pattern detection and comparison between laboratories. Geobiology. 2015 Jul;13(4):391-407. doi: 10.1111/gbi.12132. Epub 2015 Apr 1[1]PubMed PMID: 25865768; PubMed Central PMCID: PMC4676935.

[2]Babiak Z, Carlisle TL, Holmlund CE. Inhibtion of diplopterol synthesis in Tetrahymena pyriformis by a hypocholesteremic compound. Lipids. 1975 Jul;10(7):437-40. PubMed PMID: 167262.

[3] Sáenz JP, Grosser D, Bradley AS, Lagny TJ, Lavrynenko O, Broda M, Simons K. Hopanoids as functional analogues of cholesterol in bacterial membranes. Proc Natl Acad Sci U S A. 2015 Sep 22;112(38):11971-6. doi: 10.1073/pnas.1515607112. Epub 2015 Sep 8. PubMed PMID: 26351677; PubMed Central PMCID: PMC4586864.

[4] Caron B, Mark AE, Poger D. Some Like It Hot: The Effect of Sterols and Hopanoids on Lipid Ordering at High Temperature. J Phys Chem Lett. 2014 Nov 20;5(22):3953-7. doi: 10.1021/jz5020778. Epub 2014 Nov 3. PubMed PMID: 26276476.

[5] Subhash Y, Sasikala Ch, Ramana ChV. Sphingopyxis contaminans sp. nov., isolated from a contaminated Petri dish. Int J Syst Evol Microbiol. 2014 Jul;64(Pt 7):2238-43. doi: 10.1099/ijs.0.061937-0. Epub 2014 Apr 7. PubMed PMID: 24711587.

6: Subhash Y, Tushar L, Sasikala Ch, Ramana ChV. Mongoliicoccus alkaliphilus sp. nov. and Litoribacter alkaliphilus sp. nov., isolated from salt pans. Int J Syst Evol Microbiol. 2013 Sep;63(Pt 9):3457-62. doi: 10.1099/ijs.0.049924-0. Epub 2013 Mar 29. PubMed PMID: 23543498.7: Kannenberg E, Poralla K. The influence of hopanoids on growth of Mycoplasma mycoides. Arch Microbiol. 1982 Dec;133(2):100-2. PubMed PMID: 6762170.8: Subhash Y, Sasikala Ch, Ramana ChV. Flavobacterium aquaticum sp. nov., isolated from a water sample of a rice field. Int J Syst Evol Microbiol. 2013 Sep;63(Pt 9):3463-9. doi: 10.1099/ijs.0.050047-0. Epub 2013 Mar 29. PubMed PMID: 23543500.9: Lodha TD, Srinivas A, Sasikala C, Ramana CV. Hopanoid inventory of Rhodoplanes spp. Arch Microbiol. 2015 Aug;197(6):861-7. doi: 10.1007/s00203-015-1112-5. Epub 2015 May 3. PubMed PMID: 25935452.10: Sáenz JP, Sezgin E, Schwille P, Simons K. Functional convergence of hopanoids and sterols in membrane ordering. Proc Natl Acad Sci U S A. 2012 Aug 28;109(35):14236-40. doi: 10.1073/pnas.1212141109. Epub 2012 Aug 14. PubMed PMID: 22893685; PubMed Central PMCID: PMC3435179.1

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